Canonical Allele Identifier: CA410688474
Gene: COMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19962581C>A , CM000684.2:g.19962581C>A GRCh38
NC_000022.10:g.19950104C>A , CM000684.1:g.19950104C>A GRCh37
NC_000022.9:g.18330104C>A NCBI36
NG_011526.1:g.25842C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361682.11:c.55C>A MANE Select ENSP00000354511.6:p.Leu19Met
ENST00000428707.2:c.55C>A ENSP00000387695.2:p.Leu19Met
ENST00000676678.1:c.55C>A ENSP00000503719.1:p.Leu19Met
ENST00000678255.1:c.55C>A ENSP00000504402.1:p.Leu19Met
ENST00000678769.1:c.55C>A ENSP00000503289.1:p.Leu19Met
ENST00000678868.1:c.55C>A ENSP00000503583.1:p.Leu19Met
ENST00000207636.9:c.55C>A ENSP00000207636.5:p.Leu19Met
ENST00000361682.10:c.55C>A ENSP00000354511.6:p.Leu19Met
ENST00000403184.5:c.55C>A ENSP00000383966.1:p.Leu19Met
ENST00000403710.5:c.55C>A ENSP00000385917.1:p.Leu19Met
ENST00000406520.7:c.55C>A ENSP00000385150.3:p.Leu19Met
ENST00000407537.5:c.55C>A ENSP00000384654.2:p.Leu19Met
ENST00000412786.5:c.55C>A ENSP00000403958.1:p.Leu19Met
ENST00000449653.5:c.-96C>A ENSP00000416778.1:n.-96C>A
ENST00000467943.5:n.251C>A
NM_000754.3:c.55C>A NP_000745.1:p.Leu19Met
NM_001135161.1:c.55C>A NP_001128633.1:p.Leu19Met
NM_001135162.1:c.55C>A NP_001128634.1:p.Leu19Met
NM_007310.2:c.-96C>A NP_009294.1:n.-96C>A
XM_011529885.1:c.169C>A XP_011528187.1:p.Leu57Met
XM_011529886.1:c.169C>A XP_011528188.1:p.Leu57Met
XM_011529887.1:c.55C>A XP_011528189.1:p.Leu19Met
XM_011529888.1:c.55C>A XP_011528190.1:p.Leu19Met
XM_011529889.1:c.55C>A XP_011528191.1:p.Leu19Met
XM_011529890.1:c.55C>A XP_011528192.1:p.Leu19Met
XM_011529891.1:c.55C>A XP_011528193.1:p.Leu19Met
NM_001362828.1:c.55C>A NP_001349757.1:p.Leu19Met
XM_011529886.2:c.466C>A XP_011528188.2:p.Leu156Met
XM_017028595.1:c.55C>A XP_016884084.1:p.Leu19Met
NM_000754.4:c.55C>A MANE Select NP_000745.1:p.Leu19Met
NM_001135161.2:c.55C>A NP_001128633.1:p.Leu19Met
NM_001135162.2:c.55C>A NP_001128634.1:p.Leu19Met
NM_001362828.2:c.55C>A NP_001349757.1:p.Leu19Met
NM_007310.3:c.-96C>A NP_009294.1:n.-96C>A